At CHEORS, our team of PRO experts have a multidisciplinary background with research experience ranging from 5 to 30+ years. Data collection is gathered through strategic partners from global settings that can include patient reported outcome (PRO) measures, caregiver/observer-reported outcome (ObsRO) measures and clinician-reported outcome (ClinRO) measures. We are able to evaluate the role of the PRO endpoints in clinical trial by primary, key secondary, and exploratory endpoints while also developing the strategy for PRO-based labeling claims and reimbursement. CHEORS has a strong expertise in advanced statistical techniques that include item response theory, factor analysis, latent class analysis, validity and reliability assessment, and response shift assessment.
“Thank you for this. This is great work!”
Principal Scientist,
Biopharmaceutical Company“I am very happy working with the CHEORS team. CHEORS stands out in particular in the area of communication and responsiveness. I always feel assured that there is no misunderstanding.”
Assoc. Director,
Biopharmaceutical Company“I am most pleased to work with CHEORS. We managed early deadlines with high-quality end results.”
Specialist,
Outcomes Research/Medical Affairs"With aspect of technical knowledge, communication and responsiveness, CHEORS is fantastic. I am very happy with your work. Frankly, you have over-delivered than what I expected"
HTA Manager,
Biopharmaceutical Company“CHEORS is experienced and found solutions to all issues we faced during the preparation time. Communication was very precise and strict—we were happy to work with the team.”